JP2018188716A - Low alloy steel for hydrogen accumulator, and hydrogen accumulator - Google Patents

Low alloy steel for hydrogen accumulator, and hydrogen accumulator Download PDF

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JP2018188716A
JP2018188716A JP2017094893A JP2017094893A JP2018188716A JP 2018188716 A JP2018188716 A JP 2018188716A JP 2017094893 A JP2017094893 A JP 2017094893A JP 2017094893 A JP2017094893 A JP 2017094893A JP 2018188716 A JP2018188716 A JP 2018188716A
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hydrogen
low alloy
alloy steel
pressure accumulator
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JP6490141B2 (en
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祐介 柳沢
Yusuke Yanagisawa
祐介 柳沢
荒島 裕信
Hironobu Arashima
裕信 荒島
洋流 和田
Hiroharu Wada
洋流 和田
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Japan Steel Works Ltd
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Abstract

PROBLEM TO BE SOLVED: To provide a low alloy steel that is excellent in in-hydrogen fatigue limit and is suitable as a hydrogen accumulator, and provide the hydrogen accumulator using the low alloy steel.SOLUTION: A low alloy steel for a hydrogen accumulator contains, in mass%, C: 0.25-0.45%, Si: 0.05-1.0%, Mn: 0.25-2.0%, and optionally Ni: 4.0% or less, Cr: 0.6-2.0%, Mo: 0.15-0.50%, with the balance being Fe and unavoidable impurities, where in the unavoidable impurities, the content of O is 0.0030% or less. Preferably, non-metallic inclusions have a maximum size of 35 μm or less.SELECTED DRAWING: Figure 2

Description

本発明は、水素蓄圧器用の低合金鋼および該低合金鋼を用いた水素蓄圧器に関するものである。   The present invention relates to a low alloy steel for a hydrogen pressure accumulator and a hydrogen pressure accumulator using the low alloy steel.

燃料電池自動車などに水素を供給する水素ステーションでは、高圧で水素を保管する水素蓄圧器が利用されている。水素蓄圧器には高い安全性が要求され、自動車への水素充填に伴って内圧変動が生じるため、特に疲労破壊が問題となる。その一方で、蓄圧器の肉厚をなるだけ薄くして軽量・低コストとすることが要望されている。タイプ1の蓄圧器およびタイプ2の蓄圧器のライナーには、Cr−Mo鋼などの高強度低合金鋼が主に使用されているが、これらの鋼種は、高圧水素環境下においては、大気中に比べて引張強度や疲労特性が低下することが知られている。   In a hydrogen station that supplies hydrogen to a fuel cell vehicle or the like, a hydrogen pressure accumulator that stores hydrogen at a high pressure is used. The hydrogen pressure accumulator is required to have high safety, and the internal pressure fluctuates as hydrogen is charged into the automobile. On the other hand, it is desired to reduce the wall thickness of the pressure accumulator as much as possible to reduce the weight and cost. High-strength low-alloy steels such as Cr-Mo steel are mainly used for the liners of type 1 and type 2 accumulators, but these steel types are used in the atmosphere under high-pressure hydrogen environment. It is known that the tensile strength and fatigue characteristics are reduced compared to

これまでに、水素蓄圧器に関する種々の技術が検討されている。例えば、非特許文献1では、水素中における強度・疲労特性を考慮した蓄圧器の設計手法が提案されている。
非特許文献2では、高圧水素中では大気中と比べて低合金鋼の疲労寿命は低下するものの、疲労限度はほぼ同等となることが報告されている。
ただし、高圧水素環境中で鋼材の疲労限度を測定するには、特殊な試験装置を使用して長期間の試験を行う必要があるため、時間・コスト的な負荷が大きい。そのため、上記の技術においても、大気中と水素中の疲労限度が等しくなる鋼材を用いることが、蓄圧器の設計において重要であることが示されている。
So far, various technologies relating to hydrogen pressure accumulators have been studied. For example, Non-Patent Document 1 proposes a pressure accumulator design method in consideration of strength and fatigue characteristics in hydrogen.
Non-Patent Document 2 reports that the fatigue life of low-alloy steel is lower in high-pressure hydrogen than in the atmosphere, but the fatigue limit is almost the same.
However, in order to measure the fatigue limit of a steel material in a high-pressure hydrogen environment, it is necessary to perform a long-term test using a special test apparatus, so that the load in terms of time and cost is large. Therefore, it has been shown that the use of a steel material having the same fatigue limit in the atmosphere and in hydrogen is also important in the design of the pressure accumulator in the above technique.

疲労特性に注目した蓄圧器用鋼材としては、特許文献1では、金属組織を制御して、水素中の疲労限度と引張強さとの比(疲労限度/引張強さ)を0.45以上とした鋼材が提案されている。特許文献2では、金属組織と析出物とを制御して、疲労き裂進展速度を低減させた鋼材が提案されている。   As a steel material for a pressure accumulator that pays attention to fatigue characteristics, in Patent Document 1, a metal structure is controlled, and the ratio of fatigue limit to tensile strength (fatigue limit / tensile strength) in hydrogen is 0.45 or more. Has been proposed. Patent Document 2 proposes a steel material in which the metal structure and precipitates are controlled to reduce the fatigue crack growth rate.

特開2016−172969号公報Japanese Patent Laid-Open No. 2006-172969 特許第5633664号Japanese Patent No. 5633664

和田洋流ら、日本製鋼所技報、No.65(2014)、pp.36−45Y. Wada et al., Nippon Steel Works Technical Report, No. 65 (2014), pp. 36-45 宮本泰介ら、日本機械学会論文集(A編)、Vol.78、No.788(2012)、pp.531−546Taisuke Miyamoto et al., Transactions of the Japan Society of Mechanical Engineers (A), Vol. 78, no. 788 (2012), pp. 531-546

ところで、蓄圧器の疲労破壊は、水素と接する内表面を起点として生じると考えられるため、疲労特性を向上させるためには内表面に粗大な初期欠陥を生じさせないことが重要である。特に、製鋼工程において不可避的に生じる非金属介在物は疲労破壊の起点となりうるため、その影響に十分な注意を払う必要がある。
しかし、上述の従来研究において、非金属介在物に関する検討はされておらず、高圧水素環境下の鋼材の疲労特性に及ぼす非金属介在物の影響については十分にわかっていない。
By the way, since it is considered that the fatigue failure of the pressure accumulator starts from the inner surface in contact with hydrogen, it is important not to cause coarse initial defects on the inner surface in order to improve the fatigue characteristics. In particular, non-metallic inclusions that are inevitably generated in the steelmaking process can be the starting point of fatigue failure, and therefore it is necessary to pay sufficient attention to the influence.
However, in the above-described conventional research, no investigation has been made on non-metallic inclusions, and the influence of non-metallic inclusions on the fatigue characteristics of steel under high-pressure hydrogen environment is not fully understood.

本発明は上記課題を解決するためになされたものであり、水素中疲労限度が大気中疲労限度と同等となる水素蓄圧器用の低合金鋼および水素蓄圧器を提供することを目的とする。   The present invention has been made to solve the above-described problems, and an object thereof is to provide a low alloy steel for a hydrogen pressure accumulator and a hydrogen pressure accumulator whose fatigue limit in hydrogen is equivalent to the fatigue limit in air.

すなわち、本発明の水素蓄圧器用の低合金鋼のうち、第1の形態は、質量%で、C:0.25〜0.45%、Si:0.05〜1.0%、Mn:0.25〜2.0%、Cr:0.6〜2.0%、Mo:0.15〜0.50%を含有し、残部がFeおよび不可避不純物からなり、不可避不純物中でO:0.0030%以下である組成を有することを特徴とする。   That is, among the low alloy steels for the hydrogen pressure accumulator of the present invention, the first form is mass%, C: 0.25 to 0.45%, Si: 0.05 to 1.0%, Mn: 0 25 to 2.0%, Cr: 0.6 to 2.0%, Mo: 0.15 to 0.50%, and the balance is composed of Fe and inevitable impurities, and in the inevitable impurities, O: 0.0. It has the composition which is 0030% or less.

他の形態の水素蓄圧器用の低合金鋼の発明は、さらに、質量%で、Ni:4.0%以下を含有することを特徴とする。   The invention of the low alloy steel for the hydrogen pressure accumulator of another form is further characterized by containing Ni: 4.0% or less in mass%.

他の形態の水素蓄圧器用の低合金鋼の発明は、さらに、質量%で、V:0.2%以下を含有することを特徴とする。   Another aspect of the invention of the low alloy steel for a hydrogen pressure accumulator is further characterized by containing, in mass%, V: 0.2% or less.

他の形態の水素蓄圧器用の低合金鋼の発明は、前記形態の本発明において、非金属介在物の最大寸法が35μm以下であることを特徴とする   Another aspect of the invention of a low alloy steel for a hydrogen pressure accumulator is characterized in that, in the present invention of the above aspect, the maximum dimension of the nonmetallic inclusion is 35 μm or less.

他の形態の水素蓄圧器用の低合金鋼の発明は、前記形態の本発明において、焼戻しマルテンサイト組織を有することを特徴とする。   Another aspect of the invention of a low alloy steel for a hydrogen pressure accumulator according to the present invention of the above aspect is characterized by having a tempered martensite structure.

他の形態の水素蓄圧器用の低合金鋼の発明は、前記形態の本発明において、室温における引張強さが800〜1000MPaであることを特徴とする。   Another aspect of the invention of a low alloy steel for a hydrogen pressure accumulator according to the present invention of the above aspect is that the tensile strength at room temperature is 800 to 1000 MPa.

本発明の水素蓄圧器のうち、第1の形態は、前記各形態の低合金鋼を蓄圧器本体とすることを特徴とする。   Among the hydrogen pressure accumulators of the present invention, the first mode is characterized in that the low alloy steel of each of the above modes is used as a pressure accumulator body.

他の形態の水素蓄圧器の発明は、前記形態の本発明において、設計圧力範囲が40MPa以上であることを特徴とする。   Another aspect of the invention of the hydrogen pressure accumulator is characterized in that, in the present invention of the above aspect, the design pressure range is 40 MPa or more.

以下に、本発明における成分組成等の限定理由について説明する。
1.化学成分(いずれも質量%)
・C:0.25〜0.45%
Cは、鋼材の焼入れ性を向上させる元素であり、目的の強度を得るために0.25%以上の添加とする。また、Cの含有量が多すぎると焼入れ時に割れが生じる懸念があるため、含有量が0.45%以下とする。
Below, the reason for limitation, such as a component composition in this invention, is demonstrated.
1. Chemical composition (both mass%)
・ C: 0.25 to 0.45%
C is an element that improves the hardenability of the steel material, and is added at 0.25% or more in order to obtain the desired strength. Moreover, since there exists a possibility that a crack may arise at the time of hardening when there is too much content of C, content is made into 0.45% or less.

・Si:0.05〜1.0%
Siは製鋼工程における脱酸剤として使われ、非金属介在物の低減のためにも0.05%以上の含有量が必要である。しかし、多すぎるとフェライトが生成しやすくなるため、1.0%以下とする。なお、同様の理由で下限を0.05%、上限を0.35%とするのが望ましい。
・ Si: 0.05-1.0%
Si is used as a deoxidizing agent in the steelmaking process, and a content of 0.05% or more is necessary for reducing nonmetallic inclusions. However, if it is too much, ferrite tends to be generated, so the content is made 1.0% or less. For the same reason, it is desirable to set the lower limit to 0.05% and the upper limit to 0.35%.

・Mn:0.25〜2.0%
Mnは、焼入れ性を向上させ強度を高める効果があり、0.25%以上は必要である。また、多すぎると靭性を低下させるため、2.0%以下とする。なお、同様の理由で下限を0.25%、上限を1.0%とするのが望ましい。
・ Mn: 0.25 to 2.0%
Mn has the effect of improving the hardenability and increasing the strength, and 0.25% or more is necessary. Moreover, since it will reduce toughness when there is too much, it shall be 2.0% or less. For the same reason, it is desirable to set the lower limit to 0.25% and the upper limit to 1.0%.

・Ni:4.0%以下、Cr:0.6〜2.0%、Mo:0.15〜0.50%
Ni、Cr、Moはそれぞれ蓄圧器部材の焼入れ性を向上させ、強度、靭性を高めるのに有効であり、Crは0.6%以上、Moは0.15%以上の添加が必要であり、Niは、所望により含有させる。しかし、含有量が多いとコスト増の要因となるため、各元素の含有量の上限値を、Niは4.0%、Crは2.0%、Moは0.50%とする。
なお、Niを添加する場合、上記作用を得るために1.5%以上含有するのが望ましい。また、Niを不可避不純物として0.3%未満で含有してもよい。
Ni: 4.0% or less, Cr: 0.6-2.0%, Mo: 0.15-0.50%
Ni, Cr and Mo are effective for improving the hardenability of the pressure accumulator member and increasing the strength and toughness, Cr is 0.6% or more, Mo needs to be added 0.15% or more, Ni is contained as desired. However, if the content is large, the cost increases, so the upper limit of the content of each element is 4.0% for Ni, 2.0% for Cr, and 0.50% for Mo.
In addition, when adding Ni, in order to acquire the said effect | action, it is desirable to contain 1.5% or more. Ni may be contained as an inevitable impurity in an amount of less than 0.3%.

・O:0.0030%以下
OはAl、Si等と結合して非金属介在物となり、合金の疲労特性を低下させるため、その含有量を0.0030%以下とする。
O: 0.0030% or less O is combined with Al, Si, or the like to become non-metallic inclusions, and decreases the fatigue characteristics of the alloy, so its content is made 0.0030% or less.

・V:0.2%以下
Vは炭窒化物の生成を促進し、ピン止め効果により旧オーステナイト粒径の微細化に有効である。一方、0.2%を超えて含有させると焼入れ時に未固溶の炭化物が増え、焼入れ性が低下するため、その含有量を0.2%以下とする。なお、上記作用を得るために、0.05%以上含有するのが望ましい。なお、Vを不可避不純物として例えば0.01%未満で含有してもよい。
V: 0.2% or less V promotes the formation of carbonitrides and is effective for refining the prior austenite grain size due to the pinning effect. On the other hand, if the content exceeds 0.2%, undissolved carbides increase at the time of quenching, and the hardenability decreases, so the content is made 0.2% or less. In addition, in order to acquire the said effect | action, it is desirable to contain 0.05% or more. In addition, you may contain V as an inevitable impurity, for example in less than 0.01%.

2.鋼の組織・強度
・鋼の組織:焼戻しマルテンサイト組織
熱処理後の鋼の組織はマルテンサイト組織を主として有するのが望ましく、体積率で90%以上が望ましい。鋼の組織はマルテンサイト組織単相の他、疲労特性に影響しない範囲として体積率で10%以下のフェライト組織または/およびベイナイト組織が含まれてもよく、好ましくは8%以下、さらに好ましくは5%以下である。
焼入れ性が不十分でフェライト組織・ベイナイト組織が生じた場合には、疲労特性が低下する懸念がある。そのため、焼戻しマルテンサイト単層組織を有することが望ましい。ただし、疲労特性に影響しない程度の量であれば、フェライト組織または/およびベイナイト組織が含まれていてもよい。
・引張強さ:800〜1000MPa
蓄圧器の軽量化のために、鋼材の引張強さは室温で800MPa以上とするのが望ましい。しかし、強度が高すぎる場合は水素脆化が顕著に生じることから、1000MPa以下とするのが望ましい。
2. Steel structure / strength / steel structure: Tempered martensite structure The steel structure after heat treatment preferably has a martensite structure mainly, and a volume ratio of 90% or more is desirable. In addition to the single phase of martensite structure, the steel structure may include a ferrite structure and / or a bainite structure having a volume ratio of 10% or less as a range that does not affect fatigue characteristics, preferably 8% or less, more preferably 5%. % Or less.
When the hardenability is insufficient and a ferrite structure or a bainite structure is generated, there is a concern that the fatigue characteristics are lowered. Therefore, it is desirable to have a tempered martensite monolayer structure. However, a ferrite structure and / or a bainite structure may be included as long as the amount does not affect the fatigue characteristics.
-Tensile strength: 800-1000 MPa
In order to reduce the weight of the pressure accumulator, the tensile strength of the steel material is desirably 800 MPa or more at room temperature. However, when the strength is too high, hydrogen embrittlement occurs remarkably, so it is desirable that the pressure be 1000 MPa or less.

3.非金属介在物
・非金属介在物の最大寸法:35μm以下
非金属介在物は疲労破壊の起点となるため、蓄圧器の疲労寿命を著しく低下させる懸念がある。特に、大気中の疲労限度に比べて水素中の疲労限度が低下する場合には、蓄圧器の信頼性が低下する懸念がある。このため、非金属介在物の最大寸法を35μm以下とするのが望ましい。
3. Maximum dimension of non-metallic inclusions / non-metallic inclusions: 35 μm or less Since non-metallic inclusions are the starting point of fatigue failure, there is a concern that the fatigue life of the pressure accumulator will be significantly reduced. In particular, when the fatigue limit in hydrogen is lower than the fatigue limit in the atmosphere, there is a concern that the reliability of the pressure accumulator may be reduced. For this reason, it is desirable that the maximum dimension of the nonmetallic inclusion be 35 μm or less.

4.水素蓄圧器の設計圧力範囲
・設計圧力範囲:40MPa以上
水素ステーションで使用させる水素蓄圧器には、低圧用(主に40MPa未満)と高圧用(主に70MPa以上)のものがある。高圧用の蓄圧器は低圧性の蓄圧器よりも高い安全性が要求されるため、鋼材の疲労特性の要求も厳しいものとなる。本発明の低合金鋼は高圧用の蓄厚器部材への適用を想定していることから、設計圧力範囲を40MPa以上とするのが望ましい。ただし、40MPa未満での使用が排除されるものではない。
4). Design pressure range and design pressure range of hydrogen pressure accumulator: 40 MPa or more The hydrogen pressure accumulators used in the hydrogen station include those for low pressure (mainly less than 40 MPa) and for high pressure (mainly 70 MPa or more). Since high pressure accumulators require higher safety than low pressure accumulators, the demands on the fatigue characteristics of steel materials are severe. Since the low alloy steel of the present invention is assumed to be applied to a high pressure accumulator member, the design pressure range is preferably 40 MPa or more. However, use at less than 40 MPa is not excluded.

本発明によれば、高圧水素環境下における疲労限度が大気中と同等になり、水素蓄圧器の疲労試験を大気中で適切に行うことが可能となるため、水素蓄圧器の設計の信頼性と安全性を向上させることが可能となる。   According to the present invention, the fatigue limit under a high-pressure hydrogen environment is equivalent to that in the atmosphere, and the fatigue test of the hydrogen pressure accumulator can be performed appropriately in the atmosphere. It becomes possible to improve safety.

本発明の一実施形態における水素蓄圧器を示す断面図である。It is sectional drawing which shows the hydrogen pressure accumulator in one Embodiment of this invention. 本発明の実施例における、各試験片の非金属介在物の最大寸法の極値統計を示すグラフである。It is a graph which shows the extreme value statistics of the largest dimension of the nonmetallic inclusion of each test piece in the Example of this invention. 同じく、最大介在物寸法と疲労限度比との関係を示すグラフである。Similarly, it is a graph showing the relationship between the maximum inclusion size and the fatigue limit ratio. 同じく、酸素量と疲労限度比との関係を示すグラフである。Similarly, it is a graph showing the relationship between the amount of oxygen and the fatigue limit ratio.

本発明の水素蓄圧器用の低合金鋼および水素蓄圧器の一実施形態について説明する。なお、本実施形態の低合金鋼は常法により作製することができる。
低合金鋼の素材となる鋼材に対して転炉または電気炉を利用して一次精錬を行い、その後、一次精錬を経て転炉または電気炉から出鋼した溶鋼に対し、各種元素の添加および不純物の除去を行う二次精錬を実施する。これらの工程により、質量%で、C:0.25〜0.45%、Si:0.05〜1.0%、Mn:0.25〜2.0%、Ni:4.0%以下、Cr:0.6〜2.0%、Mo:0.15〜0.50%を含有し、残部がFeおよび不可避不純物からなり、不可避不純物中でO:0.0030%以下である組成を有する低合金鋼を得ることができる。さらに、所望によりV:0.2%以下を含有するもの。
One embodiment of the low alloy steel and hydrogen pressure accumulator for the hydrogen pressure accumulator of the present invention will be described. In addition, the low alloy steel of this embodiment can be produced by a conventional method.
Addition of various elements and impurities to the molten steel produced from the converter or electric furnace after primary refining using low temperature converter steel or electric furnace to the steel material used as low alloy steel Secondary refining is performed to remove By these steps, C: 0.25 to 0.45%, Si: 0.05 to 1.0%, Mn: 0.25 to 2.0%, Ni: 4.0% or less, It contains Cr: 0.6-2.0%, Mo: 0.15-0.50%, the balance is composed of Fe and inevitable impurities, and in the inevitable impurities, O: 0.0030% or less. Low alloy steel can be obtained. Furthermore, V contains 0.2% or less as desired.

なお、二次精錬では、非金属介在物の低減のために、真空脱ガス処理を含む工程によって精錬を行うことが望ましい。真空処理が適用されることで、脱ガス、脱酸、脱非金属介在物等の効果が得られる。二次精錬を経た低合金鋼に対しては鋳造を行って低合金鋼材が得られる。
なお、上記溶製は一例として示されるものであり、本願発明としては溶製方法が特に限定されるものではない。
In secondary refining, it is desirable to perform refining by a process including vacuum degassing treatment in order to reduce non-metallic inclusions. By applying the vacuum treatment, effects such as degassing, deoxidation, and non-metallic inclusions can be obtained. The low alloy steel that has undergone secondary refining is cast to obtain a low alloy steel.
The melting is shown as an example, and the melting method is not particularly limited as the present invention.

低合金材には焼入れおよび焼戻しを行う。焼入れや焼戻しの条件は特に限定されないが、例えば、800℃〜950℃で焼入れを行った後に、600〜650℃で焼戻しを行うことができる。焼入れ後に所望の形状への加工を行うことができるが、焼入れ前に形状の加工を行うことも可能である。得られた低合金鋼は焼戻しマルテンサイト組織を有しており、引張強さが800〜1000MPaとなっている。   The low alloy material is quenched and tempered. The conditions for quenching and tempering are not particularly limited. For example, after quenching at 800 ° C. to 950 ° C., tempering can be performed at 600 to 650 ° C. Although it can process to a desired shape after quenching, it is also possible to process the shape before quenching. The obtained low alloy steel has a tempered martensite structure and a tensile strength of 800 to 1000 MPa.

低合金鋼材に対しては適宜の加工を行う。例えば円筒形状にする。その製造方法は特に限定されるものではないが、欠陥の少ない加工方法が望ましく、例えば、鍛造や押し出しなどによって一体に成形するのが望ましい。   Appropriate processing is performed on the low alloy steel. For example, a cylindrical shape is used. The manufacturing method is not particularly limited, but a processing method with few defects is desirable, and for example, it is desirable to form integrally by forging or extrusion.

得られた低合金鋼は、非金属介在物の最大寸法が35μm以下となっており、高圧水素中で疲労破壊の起点となる非金属介在物の大きさが抑制されているため、高圧水素中と大気中での疲労限度が同等となっている。   The obtained low alloy steel has a maximum dimension of non-metallic inclusions of 35 μm or less, and the size of non-metallic inclusions that are the starting point of fatigue fracture in high-pressure hydrogen is suppressed. And the fatigue limit in the atmosphere is equivalent.

得られた低合金鋼は水素蓄圧器の材料として好適に使用することができる。
図1は、上記低合金鋼を用いた水素蓄圧器1を示している。蓄圧器本体2は、低合金鋼で構成されており、上記したように一体成形によって円筒形状に整形される。蓄圧器本体2の開口部3には、蓋部4を取り付けて水素蓄圧器1を構成している。なお、蓋部4は、蓄圧器本体2を構成した低合金鋼と同種の材料を用いてもよく、また、他の材料によって構成されるものであってもよい。
本実施形態の低合金鋼は高い疲労限度を有していることから高圧用の蓄圧器部材として好適であり、設計圧力範囲を40MPa以上で好適に用いることができる。
The obtained low alloy steel can be suitably used as a material for a hydrogen pressure accumulator.
FIG. 1 shows a hydrogen pressure accumulator 1 using the low alloy steel. The accumulator body 2 is made of low alloy steel, and is shaped into a cylindrical shape by integral molding as described above. A lid 4 is attached to the opening 3 of the pressure accumulator body 2 to constitute the hydrogen pressure accumulator 1. In addition, the cover part 4 may use the same kind of material as the low alloy steel which comprised the pressure accumulator main body 2, and may be comprised with another material.
Since the low alloy steel of this embodiment has a high fatigue limit, it is suitable as a pressure accumulator member for high pressure, and can be suitably used at a design pressure range of 40 MPa or more.

本実施形態によれば、高圧水素中と大気圧中とで同等の疲労限度を有する水素蓄圧器用の低合金鋼を得ることができる。   According to the present embodiment, a low alloy steel for a hydrogen pressure accumulator having an equivalent fatigue limit in high-pressure hydrogen and atmospheric pressure can be obtained.

表1に示す化学成分(残部がFeおよびその他の不純物)を有する低合金鋼A〜Gを用意した。
なお、低合金鋼は所定の成分となるように溶解後に、鍛造もしくは圧延を施して製造した。
各低合金鋼からなる供試材に対し、表2に示す条件で焼入れと焼戻しを行う熱処理を実施した。
熱処理後の供試材において、金属組織観察、非金属介在物寸法、機械特性、および疲労特性の測定を行った。
Low alloy steels A to G having chemical components shown in Table 1 (the balance being Fe and other impurities) were prepared.
The low alloy steel was manufactured by forging or rolling after melting so as to be a predetermined component.
A heat treatment for quenching and tempering was performed on the specimens made of each low alloy steel under the conditions shown in Table 2.
In the test material after the heat treatment, metal structure observation, dimensions of non-metallic inclusions, mechanical properties, and fatigue properties were measured.

(非金属介在物の寸法)
非金属介在物の測定は極値統計法で実施した。観察面は試験片の軸方向断面とした。4×5mmの領域を60視野観察し、各視野における最大サイズの非金属介在物について、その面積を楕円近似によって測定した。測定された最大サイズの非金属介在物の面積areamaxに基づいて、最大サイズの非金属介在物の寸法√(areamax)を求め、その後、各試験片における最大サイズの非金属介在物の寸法√(areamax)を図2に示す極値統計グラフに整理した。
その後、得られた結果を直線状に近似し、試験片の危険体積における最大介在物寸法の推定を行った。最大非金属介在物の寸法の測定結果を表2に示した。推定される最大介在物寸法は18〜46μmとなった。
なお、実際の蓄圧器においては、試験片で見積もった値よりも危険体積が大きな値となるが、最大介在物寸法が35μm以下となる鋼材においては、直線の傾きが大きくなるため、危険体積の違いによる影響は相対的に小さいと考えられる。
(Dimensions of non-metallic inclusions)
The measurement of nonmetallic inclusions was carried out by the extreme value statistical method. The observation surface was an axial section of the test piece. 60 fields of a 4 × 5 mm region were observed, and the area of each non-metallic inclusion having the maximum size in each field was measured by elliptic approximation. Based on the measured area max of the non-metallic inclusion of the maximum size, the dimension √ (area max ) of the non-metallic inclusion of the maximum size is obtained, and then the dimension of the non-metallic inclusion of the maximum size in each specimen √ (area max ) is arranged in the extreme value statistical graph shown in FIG.
Thereafter, the obtained result was approximated to a straight line, and the maximum inclusion size in the dangerous volume of the test piece was estimated. Table 2 shows the measurement results of the dimension of the maximum nonmetallic inclusion. The estimated maximum inclusion size was 18-46 μm.
In the actual pressure accumulator, the dangerous volume is larger than the value estimated with the test piece. However, in steel materials with a maximum inclusion size of 35 μm or less, the slope of the straight line is large, The effect of the difference is considered to be relatively small.

(機械的特性)
鋼材に対して引張試験を行い、鋼材の機械的特性として、0.2%耐力(0.2%Y.S.)(MPa)、引張強さ(T.S.)(MPa)、伸び(EL.)(%)、絞り(R.A.)(%)を測定した。引張試験片にはJIS Z 2201(1998) 14A号試験片を用いて、引張試験はJIS Z 2241(1998)に従って実施した。測定結果を表2に示した。
(Mechanical properties)
A tensile test was performed on the steel material, and the mechanical properties of the steel material were 0.2% proof stress (0.2% YS) (MPa), tensile strength (TS) (MPa), elongation ( EL.) (%) And aperture (RA) (%) were measured. A tensile test was conducted according to JIS Z 2241 (1998) using a JIS Z 2201 (1998) No. 14A test piece. The measurement results are shown in Table 2.

(疲労試験)
疲労試験は、大気中および90MPa水素中で、荷重制御で実施した。疲労波形は正弦波とし、周波数を0.5〜5Hzとした。大気中試験では300万回を、水素中試験では30万回を打ち切り回数とした。測定された大気中疲労限度(MPa)および水素中疲労限度(MPa)を表2に示した。
また、水素中と大気中との疲労特性の違いを評価するために、水素中疲労限度と大気中疲労限度との比(水素中疲労限度/大気中疲労限度)を疲労限度比として算出し、結果を表2に示した。
(Fatigue test)
The fatigue test was performed under load control in air and 90 MPa hydrogen. The fatigue waveform was a sine wave and the frequency was 0.5 to 5 Hz. The number of censoring was 3 million times in the air test and 300,000 times in the hydrogen test. The measured atmospheric fatigue limit (MPa) and hydrogen fatigue limit (MPa) are shown in Table 2.
In addition, in order to evaluate the difference in fatigue characteristics between hydrogen and the atmosphere, the ratio between the fatigue limit in hydrogen and the atmospheric fatigue limit (hydrogen fatigue limit / atmosphere fatigue limit) is calculated as the fatigue limit ratio, The results are shown in Table 2.

(金属組織観察)
金属組織観察では、焼入れ後の試料を鏡面研磨した後に、例えば、5%ピクリン酸+1%硝酸溶液を用いてエッチングし、光学顕微鏡により行った。その結果を表2に示した。
なお、ベイナイト組織の面積率0%であったものは、マルテンサイト組織単相であった。
(Metal structure observation)
In the metal structure observation, the sample after quenching was mirror-polished and then etched using, for example, a 5% picric acid + 1% nitric acid solution and an optical microscope. The results are shown in Table 2.
In addition, what was the area ratio 0% of the bainite structure was a martensite structure single phase.

Figure 2018188716
Figure 2018188716

Figure 2018188716
Figure 2018188716

表2に示すように、本発明で規定される化学成分および最大非金属介在物寸法を有する低合金鋼A〜Fからなる供試材(発明鋼)では疲労限度比が1.0となり、水素中の疲労限度が大気中と同等となっていることが確認された。一方、本発明の規定を満たしていない低合金鋼Gからなる供試材(比較鋼)では疲労限度比が0.88となり、水素中における疲労限度が低下していることが確認された。
また、最大介在物寸法√(areamax)と疲労限度比との関係を図3のグラフに示し、鋼材の酸素含有量と疲労限度比との関係を図4のグラフに示した。これらのグラフからも、最大介在物寸法が35μm以下、酸素量が0.0030%以下である、低合金鋼A〜Fからなる供試材では、水素中の疲労限度と大気中の疲労限度が等しくなっているのに対し、上記の規定を満たしていない鋼材Gでは水素中の疲労限度が低下していることが確認された。
As shown in Table 2, the test material (invention steel) composed of low alloy steels A to F having the chemical composition and maximum nonmetallic inclusion size defined in the present invention has a fatigue limit ratio of 1.0, and hydrogen. It was confirmed that the inside fatigue limit was equivalent to that in the atmosphere. On the other hand, in the test material (comparative steel) made of the low alloy steel G not satisfying the provisions of the present invention, the fatigue limit ratio was 0.88, and it was confirmed that the fatigue limit in hydrogen was lowered.
Further, the relationship between the maximum inclusion size √ (area max ) and the fatigue limit ratio is shown in the graph of FIG. 3, and the relationship between the oxygen content of the steel material and the fatigue limit ratio is shown in the graph of FIG. From these graphs, the test material made of low alloy steels A to F having a maximum inclusion size of 35 μm or less and an oxygen content of 0.0030% or less has the fatigue limit in hydrogen and the fatigue limit in the atmosphere. On the other hand, it was confirmed that the fatigue limit in hydrogen was reduced in the steel material G that did not satisfy the above-mentioned regulations.

1 水素蓄圧器
2 蓄圧器本体
4 蓋部
1 Hydrogen pressure accumulator 2 Pressure accumulator body 4 Lid

Claims (8)

質量%で、C:0.25〜0.45%、Si:0.05〜1.0%、Mn:0.25〜2.0%、Cr:0.6〜2.0%、Mo:0.15〜0.50%、を含有し、残部がFeおよび不可避不純物からなり、不可避不純物中でO:0.0030%以下である組成を有することを特徴とする水素蓄圧器用の低合金鋼。   In mass%, C: 0.25 to 0.45%, Si: 0.05 to 1.0%, Mn: 0.25 to 2.0%, Cr: 0.6 to 2.0%, Mo: A low alloy steel for a hydrogen pressure accumulator comprising 0.15 to 0.50%, the balance being Fe and inevitable impurities, and having a composition of O: 0.0030% or less in the inevitable impurities . さらに、質量%で、Ni:4.0%以下を含有することを特徴とする請求項1記載の水素蓄圧器用の低合金鋼。   The low alloy steel for a hydrogen pressure accumulator according to claim 1, further comprising Ni: 4.0% or less by mass. さらに、質量%で、V:0.2%以下を含有することを特徴とする請求項1または2に記載の水素蓄圧器用の低合金鋼。   The low alloy steel for a hydrogen pressure accumulator according to claim 1 or 2, further comprising, in mass%, V: 0.2% or less. 非金属介在物の最大寸法が35μm以下であることを特徴とする請求項1〜3のいずれか1項に記載の水素蓄圧器用の低合金鋼。   The low-alloy steel for a hydrogen pressure accumulator according to any one of claims 1 to 3, wherein the maximum dimension of the nonmetallic inclusion is 35 µm or less. 焼戻しマルテンサイト組織を有することを特徴とする請求項1〜4のいずれか1項に記載の水素蓄圧器用の低合金鋼。   The low alloy steel for a hydrogen pressure accumulator according to any one of claims 1 to 4, which has a tempered martensite structure. 室温における引張強さが800〜1000MPaであることを特徴とする請求項1〜5のいずれか一項に記載の水素蓄圧器用の低合金鋼。   The low alloy steel for a hydrogen pressure accumulator according to any one of claims 1 to 5, wherein the tensile strength at room temperature is 800 to 1000 MPa. 請求項1〜6のいずれか1項に記載の低合金鋼を蓄圧器本体とすることを特徴とする水素蓄圧器。   A hydrogen accumulator comprising the low alloy steel according to any one of claims 1 to 6 as an accumulator body. 設計圧力範囲が40MPa以上であることを特徴とする請求項7に記載の水素蓄圧器。   The hydrogen pressure accumulator according to claim 7, wherein a design pressure range is 40 MPa or more.
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